Canonical Allele Identifier: PA645411255
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro27073Ser
CA1989238
NM_001267550.2:c.81217C>T